- Bristol Myers Squibb (Cambridge, MA)
- …and in their personal lives. Read more: careers.bms.com/working-with-us . ** Associate Director , Global Regulatory Strategy, Neuroscience** **Position Summary:** ... candidate will have leadership responsibility for global regulatory strategy within a development team (DT). Serve as team lead or co-lead of marketing application… more
- Otsuka America Pharmaceutical Inc. (Boston, MA)
- …Center at: https://www.ic3.gov , or your local authorities. Otsuka America Pharmaceutical Inc., Otsuka Pharmaceutical Development & Commercialization, ... structure and function of the product labeling + Fundamental understanding of the pharmaceutical industry drug development process Preferred: + Able to work… more
- Rhythm Pharmaceuticals (Boston, MA)
- …barriers, together. Opportunity Overview Rhythm seeks an experienced and highly motivated Associate Director of Medical Writing (MW) who can independently ... develop as well as oversee the development and advancement of clinical, regulatory, medical and safety documents spanning across the development lifecycle. This… more
- Otsuka America Pharmaceutical Inc. (Boston, MA)
- …management experience, will support position at entry ( Associate Director / Director ). + An advanced understanding of drug development principles and ... research experience (as a general guideline, 1-3 years for Associate Director level; 3-6 years for ...at: https://www.ic3.gov , or your local authorities. Otsuka America Pharmaceutical Inc., Otsuka Pharmaceutical Development … more
- Takeda Pharmaceuticals (Boston, MA)
- …in order to bring life-changing therapies to patients worldwide. Join Takeda as Associate Director , Global Labeling Lead where you will be responsible for ... the development and implementation of labeling content and strategy of...(MSc, PhD, or PharmD) preferred. + 8+ years of pharmaceutical industry experience. This is inclusive of 6 years… more
- Takeda Pharmaceuticals (Boston, MA)
- …what is possible in order to bring life-changing therapies to patients worldwide. As Associate Director , Global Labeling Devices, you will be responsible for the ... development , maintenance, and implementation of Instruction for Use (IFU)...(MSc, PhD, or PharmD) preferred. + 8+ years of pharmaceutical industry experience. This is inclusive of 6 years… more
- Takeda Pharmaceuticals (Boston, MA)
- …computation platforms within the Takeda portfolio and is responsible for the day-to-day development and alignment of delivery to the strategic vision. This role is ... a best practice/quality resource. **ACCOUNTABILITIES:** + Lead the analysis, design, development , and implementation of scientific research and development data… more
- AbbVie (Worcester, MA)
- …an industry-leading data and digital strategy for biologics process and analytics development . + Build and develop leadership and technical skills in a diverse ... life sciences or science-based informatics with 10+ years of pharmaceutical industry experience. + Minimum of 8 years of...to leverage AI and ML techniques for biologics CMC development to optimize processes, improve data analysis, and enhance… more
- Takeda Pharmaceuticals (Boston, MA)
- …in Takeda's operational execution of clinical research. + Assist with the development of new and effective strategies to diversify clinical trial populations that ... Accountable for directing delivery of quality pilot programs, and business case development for broader adoption of diversity and inclusion strategies. + Collaborate… more
- Takeda Pharmaceuticals (Boston, MA)
- …Affairs Oncology Training Lead. + Responsible for identification of learning needs, development and execution of strategic, tailored training plans and packages, and ... packages and plans to address those needs + Lead development and updating of high-quality medical affairs education and...experts on Takeda Oncology products + Collaborate with the Director of Heme-Onc and Pipeline Disease & Product Training… more